Primary Device ID | 00091966041848 |
NIH Device Record Key | 48fff2f8-1abe-4749-88a5-b8569a9a37d1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AAA |
Version Model Number | 4184AAA |
Company DUNS | 944953959 |
Company Name | LIFELINE FIRST AID, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 5037833724 |
orders@lifelinefirstaid.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00091966041848 [Primary] |
LRR | First Aid Kit With Drug |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-02-17 |
Device Publish Date | 2020-02-07 |
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